Canonical Allele Identifier: PA2499240025
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1065099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Glu1517Lys
CA406958778
NM_001145809.2:c.4549G>A